siRNA delivery into human T cells and primary cells with carbon-nanotube transporters

Angew Chem Int Ed Engl. 2007;46(12):2023-7. doi: 10.1002/anie.200604295.

Authors

Zhuang Liu¹, Mark Winters, Mark Holodniy, Hongjie Dai

Affiliation

¹ Department of Chemistry, Stanford University, Stanford, CA 94305, USA.

PMID: 17290476
DOI: 10.1002/anie.200604295

No abstract available

Publication types

Research Support, N.I.H., Extramural

MeSH terms

Biosensing Techniques*
CD4 Antigens / metabolism
Drug Delivery Systems
Humans
Leukemia-Lymphoma, Adult T-Cell / genetics
Nanotubes, Carbon / chemistry*
Polyethylene Glycols / chemistry
RNA, Small Interfering / administration & dosage*
RNA, Small Interfering / pharmacology
Receptors, CCR5 / metabolism
Receptors, CXCR4 / antagonists & inhibitors*
Receptors, CXCR4 / genetics
Receptors, CXCR4 / metabolism
T-Lymphocytes / metabolism

Substances

CD4 Antigens
Nanotubes, Carbon
RNA, Small Interfering
Receptors, CCR5
Receptors, CXCR4
Polyethylene Glycols